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Pulmonary Rehabilitation in Interstitial Lung Diseases

Effects of Pulmonary Rehabilitation in Interstitial Lung Diseases: a Prospective Randomized Controlled Trial

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00882817
Enrollment
60
Registered
2009-04-17
Start date
2009-04-30
Completion date
2011-11-30
Last updated
2013-08-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Interstitial Lung Disease

Keywords

ILD

Brief summary

Treatment in interstitial lung diseases (ILD) is frequently ineffective. Pulmonary rehabilitation (PR) is an excellent therapeutic option in another chronic lung diseases such as chronic obstructive pulmonary disease (COPD). This prospective randomized controlled study aims to evaluate the short and long-term effects of PR in patients with ILD. For this purpose, 60 ILD patients will be randomly assigned to a PR or a control group. The investigators hypothesize that PR will improve exercise capacity, increase muscle force, reduce dyspnea and improve quality of life and daily life activities in ILD patients.

Interventions

OTHERPulmonary Rehabilitation

The intervention group will perform a 6 month pulmonary rehabilitation program which consists of training, patient education, nutrition counseling and psychosocial support. They will be evaluated with some tests for the study.

Sponsors

KU Leuven
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Diagnosis of interstitial lung disease according to internationally established criteria * Dyspnea on exertion * Stable medical therapy * Stable clinical condition at inclusion, with no infection or exacerbation in the previous 4 weeks

Exclusion criteria

* Co-morbidities that do not allow exercise training (unstable angina, recent myocardial infarction or cerebrovascular accident, active cancer, severe orthopedic disorders). * Life expectancy below 3 months

Design outcomes

Primary

MeasureTime frameDescription
changes in six minute walking distance after 6 months6 monthsprimary outcome of rehabilitation programm

Secondary

MeasureTime frame
Change in peripheral and respiratory muscle force3-6-12 months
Change in maximal exercise capacity3-6-12 months
Change in daily physical activity measured by Sensewear armband3-6-12 months
Changes in pulmonary function and blood gases at rest3-6-12 months
Changes in dyspnea and quality of life scores (MMRC, CRDQ, SGRQ),3-6-12 months
Change in functional exercise capacity measured by the 6 minute walking distance12 months
To evaluate feasibility and safety of pulmonary rehabilitation in interstitial lung disease6 months
Changes in six minute walking distanceat 3, 12 months
Change number of disease-related hospitalizations and survival3-6-12 months

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 5, 2026